Anand Swaroop


Ontology type: schema:Person     


Person Info

NAME

Anand

SURNAME

Swaroop

Publications in SciGraph latest 50 shown

  • 2022-03-21 GATD3A, a mitochondrial deglycase with evolutionary origins from gammaproteobacteria, restricts the formation of advanced glycation end products in BMC BIOLOGY
  • 2021-04-14 Making Biological Sense of Genetic Studies of Age-Related Macular Degeneration in AGE-RELATED MACULAR DEGENERATION
  • 2020-04-15 Pharmacologic fibroblast reprogramming into photoreceptors restores vision in NATURE
  • 2020-03-25 Retinal Organoids derived from hiPSCs of an AIPL1-LCA Patient Maintain Cytoarchitecture despite Reduced levels of Mutant AIPL1 in SCIENTIFIC REPORTS
  • 2020-02-14 Deep-learning-based prediction of late age-related macular degeneration progression in NATURE MACHINE INTELLIGENCE
  • 2019-05-08 Author Correction: Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration in NATURE GENETICS
  • 2019-02-11 Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration in NATURE GENETICS
  • 2018-03-22 Determination of Mitochondrial Oxygen Consumption in the Retina Ex Vivo: Applications for Retinal Disease in MOUSE RETINAL PHENOTYPING
  • 2017-03-14 Nrl knockdown by AAV-delivered CRISPR/Cas9 prevents retinal degeneration in mice in NATURE COMMUNICATIONS
  • 2016-08-29 Next-generation genotype imputation service and methods in NATURE GENETICS
  • 2015-12-21 A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants in NATURE GENETICS
  • 2015-08-26 Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies in SCIENTIFIC REPORTS
  • 2014-06-20 Ciliopathy-associated gene Cc2d2a promotes assembly of subdistal appendages on the mother centriole during cilia biogenesis in NATURE COMMUNICATIONS
  • 2014-03-22 Photoreceptor Degeneration: Molecular Mechanisms of Photoreceptor Degeneration in VERTEBRATE PHOTORECEPTORS
  • 2014-03-16 Ancestry estimation and control of population stratification for sequence-based association studies in NATURE GENETICS
  • 2013-10-11 Genetic architecture of retinal and macular degenerative diseases: the promise and challenges of next-generation sequencing in GENOME MEDICINE
  • 2013-09-15 Identification of a rare coding variant in complement 3 associated with age-related macular degeneration in NATURE GENETICS
  • 2013-09-04 Genome-wide association study and meta-analysis of intraocular pressure in HUMAN GENETICS
  • 2013-05-07 An isoform of retinoid-related orphan receptor β directs differentiation of retinal amacrine and horizontal interneurons in NATURE COMMUNICATIONS
  • 2012-12-15 A role for prenylated rab acceptor 1 in vertebrate photoreceptor development in BMC NEUROSCIENCE
  • 2012-12-03 Photoreceptor sensory cilia and ciliopathies: focus on CEP290, RPGR and their interacting proteins in CILIA
  • 2012-11-16 CEP290 is required for photoreceptor ciliogenesis and other cilia related functions in CILIA
  • 2012-11-16 Reciprocal rescue of sensory cell cilia defects by Cep290 and Mkks alleles in CILIA
  • 2012-05-10 Retinal Transcriptome Profiling by Directional Next-Generation Sequencing Using 100 ng of Total RNA in RETINAL DEVELOPMENT
  • 2012-05-10 Exome Sequencing: Capture and Sequencing of All Human Coding Regions for Disease Gene Discovery in RETINAL DEVELOPMENT
  • 2012-05-10 Determination of Posttranslational Modifications of Photoreceptor Differentiation Factor NRL: Focus on SUMOylation in RETINAL DEVELOPMENT
  • 2010-08 Transcriptional regulation of photoreceptor development and homeostasis in the mammalian retina in NATURE REVIEWS NEUROSCIENCE
  • 2010-07 Associations of CFHR1–CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent in NATURE GENETICS
  • 2009-12-31 RPGR-containing protein complexes in syndromic and non-syndromic retinal degeneration due to ciliary dysfunction in JOURNAL OF GENETICS
  • 2009-12-28 Multiprotein Complexes of Retinitis Pigmentosa GTPase Regulator (RPGR), a Ciliary Protein Mutated in X-Linked Retinitis Pigmentosa (XLRP) in RETINAL DEGENERATIVE DISEASES
  • 2009-11-06 Long-term follow-up of a family with dominant X-linked retinitis pigmentosa in EYE
  • 2009-05-10 A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies in NATURE GENETICS
  • 2009-01-09 Canine RD3 mutation establishes rod-cone dysplasia type 2 (rcd2) as ortholog of human and murine rd3 in MAMMALIAN GENOME
  • 2008 Retinal Phenotype of an X-Linked Pseudo-usher Syndrome in Association with the G173R Mutation in the RPGR Gene in RECENT ADVANCES IN RETINAL DEGENERATION
  • 2006-11 Retinal repair by transplantation of photoreceptor precursors in NATURE
  • 2006-08-27 CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration in NATURE GENETICS
  • 2006-05-07 The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4 in NATURE GENETICS
  • 2005-11-28 Gene expression signatures and biomarkers of noninvasive and invasive breast cancer cells: comprehensive profiles by representational difference analysis, microarrays and proteomics in ONCOGENE
  • 2005-06-01 Mechanisms of aging in senescence-accelerated mice in GENOME BIOLOGY
  • 2005-02-20 Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin in NATURE GENETICS
  • 2004-01-21 Multicriteria Gene Screening for Analysis of Differential Expression with DNA Microarrays in EURASIP JOURNAL ON ADVANCES IN SIGNAL PROCESSING
  • 2003-09-22 Annotation and analysis of 10,000 expressed sequence tags from developing mouse eye and adult retina in GENOME BIOLOGY
  • 2002-07-30 Transcriptome analysis of the retina in GENOME BIOLOGY
  • 2001-11-05 Nrl is required for rod photoreceptor development in NATURE GENETICS
  • 2001 X-Linked Retinitis Pigmentosa: Current Status in NEW INSIGHTS INTO RETINAL DEGENERATIVE DISEASES
  • 2000-10-03 NRL S50T mutation and the importance of ‘founder effects’ in inherited retinal dystrophies in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1999-04 A mutation in NRL is associated with autosomal dominant retinitis pigmentosa in NATURE GENETICS
  • 1996 Rapid YAC End Sequencing by Alu-Vector PCR and Biotinylated Primers in A LABORATORY GUIDE TO BIOTIN-LABELING IN BIOMOLECULE ANALYSIS
  • 1995-04 Dinucleotide polymorphism at the DXS1178 locus is tightly linked to PGK1 at Xq13 in HUMAN GENETICS
  • 1994 A Sandwich-Hybridization Method for Specific and Efficient Selection of cDNA Clones from Genomic Regions in IDENTIFICATION OF TRANSCRIBED SEQUENCES
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